Actively Recruiting
Evaluation and Management of Cardio Toxicity in Oncologic Patients
Led by Tel-Aviv Sourasky Medical Center · Updated on 2022-02-02
1000
Participants Needed
1
Research Sites
804 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The survival rate of cancer patients has greatly increased over the past decades' mainly due to early detection and the use of new medications with higher doses and combined protocols. This achievement comes with the price of cardio toxicity, leading to cardiac dysfunction ranged from transient asymptomatic left ventricular dysfunction to cardiac death. In the long term, the risk of death from cardiovascular causes exceeds that of tumor recurrence for many types of cancer. As a result of the increasing number of long-term cancer survivors the magnitude of this problem is growing. Early identification of cardio toxicity can be identified by clinical follow-up and the use of electrocardiography, cardiac biomarkers (Troponin, brain natriuretic peptide) and echocardiogram. Past studies imply that the addition of angiotensin-converting-enzyme inhibitor (ACE inhibitor) and beta blockers to the patient's treatment may prevent the development of cardiac dysfunction. However, currently there are no specific or clear guidelines for the follow-up and management of cardio-toxicity in cancer patients. The aim of the study: To try to identify who are the patients at increased risk for developing cardio toxicity, by follow up of clinical evaluation, cardiac biomarkers and echocardiogram examination, in purpose of early diagnosis, management and prevention of cardiac events. For achieving this the investigators will build a registry which will include all the oncologic patients going an evaluation in the cardio-oncology clinic in the Tel Aviv Medical Center .
CONDITIONS
Official Title
Evaluation and Management of Cardio Toxicity in Oncologic Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients evaluated in the cardio-oncology clinic in Tel Aviv Medical Center
You will not qualify if you...
- Patients in the prospective study who do not sign an informed consent form
- Patients who choose to stop participating in the study
AI-Screening
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Trial Site Locations
Total: 1 location
1
Tel Aviv Medical Center
Tel Aviv, Israel
Actively Recruiting
Research Team
M
Michal Laufer Perl, MD
CONTACT
U
Udi Chorin, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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